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利用白菜 bulked segregant sequencing 技术鉴定出控制根肿病抗性的两个 QTL。

Two QTLs controlling Clubroot resistance identified from Bulked Segregant Sequencing in Pakchoi (Brassica campestris ssp. chinensis Makino).

机构信息

Shanghai Key Lab of Protected Horticultural Technology, Horticultural Research Institute, Shanghai Academy of Agricultural Sciences, Shanghai, 201106, China.

出版信息

Sci Rep. 2019 Jun 25;9(1):9228. doi: 10.1038/s41598-019-44724-z.

Abstract

Clubroot, caused by Plasmodiophora Brassicae, is a serious soil-borne disease in worldwide. In recent years, progression of clubroot is rapid and serious in Shanghai, China. In this study, The inheritance of clubroot resistance (CR) were determined in pakchoi using F segregation population that were developed by crossing highly resistant line 'CR38' and susceptible line 'CS22'. Two novel QTLs, qBrCR38-1 and qBrCR38-2, was identified by BSA-seq (Bulked Segregant Sequencing) resistant to P. brassicae physiological race 7. Two significant peak qBrCR38-1 and qBrCR38-2 were observed by three statistical methods between interval of 19.7-20.6 Mb in chromosome A07 and 20.0-20.6 Mb in chromosome A08, respectively. In addition, Polymorphic SNPs identified within target regions were converted to kompetitive allele-specific PCR (KASP) assays. In target regions of qBrCR38-1 and qBrCR38-2, there were twenty SNP sites identified, eleven KASP markers of which are significantly associated to CR (P < 0.05). Seven candidate genes were identified and found to be involved in disease resistance (TIR-NBS-LRR proteins), defense responses of bacterium and fungi and biotic/abiotic stress response in the target regions harboring the two QTLs. Two novel QTLs and candidate genes identified from the present study provide insights into the genetic mechanism of CR in B.rapa, and the associated SNPs can be effectively used for marker-assisted breeding.

摘要

根肿病由芸薹根肿菌引起,是一种世界性的严重土传病害。近年来,中国上海根肿病的发展迅速且严重。本研究利用高抗品种‘CR38’和感病品种‘CS22’杂交构建的分离群体,鉴定了白菜根肿病抗性(CR)的遗传。通过 BSA-seq( bulked segregant sequencing )鉴定到两个与芸薹根肿菌生理小种 7 抗源相关的新 QTL,qBrCR38-1 和 qBrCR38-2。在染色体 A07 的 19.7-20.6 Mb 区间和染色体 A08 的 20.0-20.6 Mb 区间,通过三种统计方法观察到两个显著的 qBrCR38-1 和 qBrCR38-2 峰值。此外,在目标区域内鉴定出的多态性 SNP 被转化为竞争性等位基因特异性 PCR(KASP)分析。在 qBrCR38-1 和 qBrCR38-2 的目标区域内,共鉴定出 20 个 SNP 位点,其中 11 个 KASP 标记与 CR 显著相关(P < 0.05)。在包含这两个 QTL 的目标区域中,鉴定到 7 个候选基因,这些基因参与了疾病抗性(TIR-NBS-LRR 蛋白)、细菌和真菌防御反应以及生物/非生物胁迫反应。本研究从白菜中鉴定到的两个新 QTL 和候选基因,为白菜 CR 的遗传机制提供了新的见解,相关 SNP 可有效用于标记辅助育种。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4fd/6592919/994d9826aff8/41598_2019_44724_Fig1_HTML.jpg

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